@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_head
{
this:
np:hasAssertion
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion
;
np:hasProvenance
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance
;
np:hasPublicationInfo
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion
a
np:Assertion
.
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance
a
np:Provenance
.
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion
{
miriam-gene:7040
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN8112217179ae40dd1d621de0fe989516
sio:SIO_000628
miriam-gene:7040
,
lld:C0022658
;
a
sio:SIO_001122
.
}
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_provenance
{
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_assertion
dcterms:description
"[ Our study suggests that the haplotype reconstruction of TGF-beta1 gene polymorphisms could be more informative than the investigation of single nucleotide polymorphisms for defining the associated risk of developing IgAN. Further research is needed on larger cohorts to confirm TGF-beta1 involvement and test other TGF-beta1 variants with possible additive or synergistic effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15593052
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP50647.RAePmQyfpbhhg7BcfG0UNV4RVNjWTas-NsbOcXri4l_pA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}